Shibata Takahiro, Shimizu Kazuma, Hirano Keita, Nakashima Fumie, Kikuchi Ryosuke, Matsushita Tadashi, Uchida Koji
Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601; PRESTO, Japan Science and Technology Agency, Kawaguchi, Saitama 332-0012.
Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya 464-8601.
J Biol Chem. 2017 May 19;292(20):8223-8235. doi: 10.1074/jbc.M116.762609. Epub 2017 Mar 24.
Lipid peroxidation is an endogenous source of aldehydes that gives rise to covalent modification of proteins in various pathophysiological states. In this study, a strategy for the comprehensive detection and comparison of adducts was applied to find a biomarker for lipid peroxidation-modified proteins This adductome approach utilized liquid chromatography with electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) methods designed to detect the specific product ions from positively ionized adducts in a selected reaction monitoring mode. Using this procedure, we comprehensively analyzed lysine and histidine adducts generated in the oxidized low-density lipoproteins (LDL) and observed a prominent increase in several adducts, including a major lysine adduct. Based on the high resolution ESI-MS of the adduct and on the LC-ESI-MS/MS analysis of the synthetic adduct candidates, the major lysine adduct detected in the oxidized LDL was identified as -(8-carboxyoctanyl)lysine (COL). Strikingly, a significantly higher amount of COL was detected in the sera from atherosclerosis-prone mice and from patients with hyperlipidemia compared with the controls. These data not only offer structural insights into protein modification by lipid peroxidation products but also provide a platform for the discovery of biomarkers for human diseases.
脂质过氧化是醛类的内源性来源,在各种病理生理状态下会导致蛋白质的共价修饰。在本研究中,应用了一种用于加合物综合检测和比较的策略,以寻找脂质过氧化修饰蛋白的生物标志物。这种加合物组学方法利用液相色谱与电喷雾电离串联质谱(LC-ESI-MS/MS)方法,设计用于在选择反应监测模式下检测正离子化加合物的特定产物离子。使用该程序,我们全面分析了氧化型低密度脂蛋白(LDL)中产生的赖氨酸和组氨酸加合物,并观察到几种加合物显著增加,包括一种主要的赖氨酸加合物。基于加合物的高分辨率ESI-MS以及合成加合物候选物的LC-ESI-MS/MS分析,在氧化型LDL中检测到的主要赖氨酸加合物被鉴定为ε-(8-羧基辛基)赖氨酸(COL)。令人惊讶的是,与对照组相比,在易患动脉粥样硬化的小鼠和高脂血症患者的血清中检测到的COL量显著更高。这些数据不仅提供了关于脂质过氧化产物对蛋白质修饰的结构见解,还为发现人类疾病的生物标志物提供了一个平台。